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5-Bromo-4,6-dimethyl-3-pyridinecarbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63644-86-0

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63644-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63644-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,4 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63644-86:
(7*6)+(6*3)+(5*6)+(4*4)+(3*4)+(2*8)+(1*6)=140
140 % 10 = 0
So 63644-86-0 is a valid CAS Registry Number.

63644-86-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-4,6-dimethylnicotinonitrile

1.2 Other means of identification

Product number -
Other names 6-amino-3-bromo-5-nitro-2,4-lutidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:63644-86-0 SDS

63644-86-0Relevant academic research and scientific papers

ROR NUCLEAR RECEPTOR MODULATORS

-

Page/Page column 76; 77, (2016/12/26)

The invention provides compounds of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treating immunological conditions.

A General Synthesis of 5-Arylnicotinates

Thompson, Wayne J.,Gaudino, John

, p. 5237 - 5243 (2007/10/02)

Arylboronic acids have been found to couple efficiently with 5-bromonicotinates to yield 5-arylnicotinates.The reaction is considerably more sensitive to steric inhibition in the arylboronic acid component than in the pyridyl bromide 4.The dianion salt of the boronic acid is implicated as the reactive intermediate responsible for the facile coupling reaction.Pure arylboronic acids are best prepared by using triisopropyl borate as the transmetalating agent.

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